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米卡芬净用于异基因造血干细胞移植受者的抗真菌预防:临床实践中不同剂量水平的结果

Micafungin as antifungal prophylaxis in recipients of allogeneic hematopoietic stem cell transplantation: results of different dosage levels in clinical practice.

作者信息

Langebrake Claudia, Rohde Holger, Lellek Heinrich, Wolschke Christine, Kröger Nicolaus M

机构信息

Department of Stem Cell Transplantation, University Medical Center Hamburg-Eppendorf, Hamburg, Germany; Department of Pharmacy, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.

出版信息

Clin Transplant. 2014 Mar;28(3):286-91. doi: 10.1111/ctr.12310. Epub 2014 Jan 30.

Abstract

Micafungin has been approved for the prophylaxis of Candida infections in patients undergoing allogeneic hematopoietic stem cell transplantation (allo-HSCT). Here, we report a single-center experience of three different dose levels regarding efficacy, toxicity, and colonization with Candida ssp. in clinical practice. In total, 150 consecutive adult patients who underwent allo-HSCT received micafungin at a dosage of 50, 100, or 150 mg once daily for primary antifungal prophylaxis. Of those patients receiving more than six d of micafungin prophylaxis, 12/46 (26%), 6/44 (14%), and 9/46 (20%) were switched to empiric antifungal treatment. The frequency of invasive fungal infections (IFIs) according to EORTC criteria did not differ significantly (7/46; 15% vs. 5/44; 11% vs. 5/46; 11%) across the different dosage groups. In the 50-mg group, there was one case of candidemia with C. parapsilosis after 12 d of micafungin prophylaxis. In all three groups, micafungin prophylaxis was well tolerated without any case of toxicity-related treatment discontinuation. Renal function was not significantly altered, while increase of bilirubin was mainly due to concomitant ATG application. The incidence of IFIs is similar irrespective of the micafungin dosage while there was a trend toward more frequent change to empiric antifungal treatment as well as oropharyngeal colonization with candida in the lowest dosage group.

摘要

米卡芬净已被批准用于预防接受异基因造血干细胞移植(allo-HSCT)患者的念珠菌感染。在此,我们报告了在临床实践中关于三种不同剂量水平的米卡芬净在疗效、毒性以及念珠菌属定植方面的单中心经验。总共150例连续接受allo-HSCT的成年患者接受米卡芬净,剂量为每日一次50、100或150毫克,用于主要抗真菌预防。在那些接受米卡芬净预防超过6天的患者中,分别有12/46(26%)、6/44(14%)和9/46(20%)的患者转为经验性抗真菌治疗。根据欧洲癌症研究与治疗组织(EORTC)标准,不同剂量组的侵袭性真菌感染(IFI)发生率无显著差异(7/46;15% 对比 5/44;11% 对比 5/46;11%)。在50毫克组中,米卡芬净预防12天后有1例近平滑念珠菌血症。在所有三个组中,米卡芬净预防耐受性良好,没有因毒性相关而停药的情况。肾功能没有显著改变,而胆红素升高主要归因于同时应用抗胸腺细胞球蛋白(ATG)。无论米卡芬净剂量如何,IFI的发生率相似,而最低剂量组中转为经验性抗真菌治疗以及口腔念珠菌定植的频率有增加趋势。

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